The present invention provides a positive electrode for non-aqueous electrolyte secondary battery, having a novel overcharge protective function. The positive electrode for non-aqueous electrolyte secondary battery according to the present invention includes a positive electrode active material layer including a plurality of positive electrode active material particles, wherein the positive electrode active material layer comprises: a carbonaceous coating film formed on a surface of each of the positive electrode active material particles; and 0% by weight or more and 20% by weight or less of a conductive auxiliary agent disposed between the plurality of positive electrode active material particles, and at least one of the carbonaceous coating film and the conductive auxiliary agent is graphitizable carbon.

Provided is a battery comprising a cathode, an anode, and an electrolyte layer. The electrolyte layer includes a first electrolyte layer and a second electrolyte layer. The first electrolyte layer includes a first solid electrolyte material. The second electrolyte layer includes a second solid electrolyte material which is different from the first solid electrolyte material. The first solid electrolyte material includes lithium, at least one kind selected from the group consisting of metalloid elements and metal elements other than lithium, and at least one kind selected from the group consisting of chlorine and bromine. The first solid electrolyte material does not include sulfur.

A sulfur-carbon composite including a porous carbon material; and sulfur present in at least a part of pores of the porous carbon material and on an outer surface of the porous carbon material, wherein an inner surface and the outer surface of the porous carbon material are doped with a carbonate compound. Also, a positive electrode and a secondary battery including the same. Further, a method of preparing a sulfur-carbon composite and a method of preparing a positive electrode.

A stabilized lithium metal oxide cathode material comprises microparticles of lithium metal oxide in which individual particles thereof a core of lithium metal oxide and a coating of a different lithium metal oxide surrounding the core. There is an interface layer between the cores and the coatings in which there are gradients of metal ions in the direction of coating to core. The materials are made by a three stage process involving coprecipitating precursor metal hydroxide core particles at a controlled pH; coprecipitating a different metal hydroxide coating on the particles without controlling the pH; and then calcining the resulting coated precursor particles with lithium hydroxide to form the stabilized lithium metal oxide material.

A method is for producing electrochemical energy storage devices utilizing lithium and for producing materials used in the devices, such that the anode has lithium metal, inorganic solid electrolytes. Anode and cathode components are joined together by pressure and/or temperature utilized in the production. The lithium-metal layer is produced at least partly by a pulsed laser deposition method. The method can utilise various inorganic solid electrolytes produced by different methods and a roll-to-roll method as well as different ways to couple pressure and/or temperature to the component being processed.

Provided is a binder composition for a non-aqueous secondary battery electrode that can form a slurry composition for a non-aqueous secondary battery electrode having excellent viscosity stability and a non-aqueous secondary battery having excellent cycle characteristics. The binder composition for a non-aqueous secondary battery electrode contains: a polymer that includes a monomer unit including a functional group that is bondable with a cationic group and a (meth)acrylic acid ester monomer unit; and an organic compound that includes at least two cationic groups. The binder composition for a non-aqueous secondary battery electrode has a viscosity change rate of 400% or less when left at rest at a temperature of 60° C. for 30 days.

A method for producing a porous film having a water content percentage of less than 1000 ppm, the method including the steps of: (1) obtaining a porous film (A) having a water content percentage of not less than 1000 ppm; (2) obtaining a package by causing the obtained porous film (A) and a drying agent to be contained in a water vapor barrier packaging container and sealing the water vapor barrier packaging container; and (3) storing the obtained package.

An electrolytic solution for a non-aqueous electrolyte battery is provided, which is capable of providing an excellent low-temperature output characteristic at −30° C. or lower and an excellent cycle characteristic at high temperatures of 45° C. or higher. For example, the electrolytic solution contains the following salt having a divalent imide anion.

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wherein R.sup.1 to R.sup.3 represent a fluorine atom or an alkoxy group, for example, and M.sup.1 and M.sup.2 represent protons or metal cations, for example.

An effectively solvent-free alkali metal or alkali earth metal closo-borate salt is prepared in the presence of a non-aqueous solvent where the solvent can be removed to levels below one mole percent of the salt. The process involves the exchange of cations with a closo-borate anion via an acid-base process or a metathesis process. The solvent is removed from the alkali metal or alkali earth metal closo-borate salt by heating. The temperature can be greater than the melting point of the salt but lower than temperatures where decomposition occurs.

The present invention relates to an energy storage device comprising a silicate comprises a formula:
M.sub.vM1.sub.wM2.sub.xSi.sub.yO.sub.z
where M is selected from the group consisting of Li, Na, K, Al, and Mg M1 is selected from the group consisting of alkaline metals, alkaline earth metals, Ti, Mn, Fe, La, Zr, Ce, Ta, Nb, V and combinations thereof; M2 is selected from the group consisting of B, Al, Ga, Ge or combinations thereof; v, y and z are greater than 0; w and/or x is greater than 0; y≥x; and wherein M.sub.vM1.sub.wM2.sub.xSi.sub.yO.sub.z accounts for at least 90 wt % of the composition.